chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8117459613117459614GA37GENICheterozygous812871558
8117460914117460915GT22GENIChomozygous812871559
8117462354117462355CT24GENIChomozygous812871560
8117463142117463143AG11GENIChomozygous812871561
8117463763117463764CT29GENIChomozygous812871562
8117464395117464396CG5GENIChomozygous812871563
8117464601117464602TC26GENIChomozygous812871564
8117464876117464877GA14GENIChomozygous812871565
8117466249117466250AC38GENIChomozygous812871566
8117466513117466514TC25GENIChomozygous812871567
8117467952117467953AG25GENIChomozygous812871568
8117468441117468442GA16GENIChomozygous812871569
8117468564117468565GA19GENIChomozygous812871570
8117468864117468865CG19GENIChomozygous812871571
8117469362117469363TC31GENIChomozygous812871572
8117470014117470015TC23GENIChomozygous812871573
8117470387117470388GA9GENIChomozygous812871574
8117471283117471284TC36GENIChomozygous812871575
8117471357117471358AT38GENIChomozygous812871576
8117471931117471932TG25GENIChomozygous812871577
8117471948117471949GT21GENICheterozygous812871578
8117472015117472016TC41GENICheterozygous812871579
8117473215117473216GA15GENIChomozygous812871580
8117473789117473790AG16GENICheterozygous812871581
8117473918117473919AT46GENICheterozygous812871582
8117473986117473987CT60GENICheterozygous812871583
8117474100117474101AT99GENICheterozygous812871584
8117474103117474104CT94GENICheterozygous812871585
8117474142117474143TG72GENICheterozygous812871586
8117474146117474147TG69GENICheterozygous812871587
8117474153117474154GC61GENICheterozygous812871588
8117474159117474160CG57GENICheterozygous812871589
8117474164117474165TC53GENICheterozygous812871590
8117475110117475111CA39GENIChomozygous812871591